A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686465



Internal ID21208322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63101737..63101737hg38UCSC Ensembl
chr20:61733089..61733089hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803354
Supporting Variants
Samples
Known GenesHAR1A, HAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686465
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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